Polyimide for FOLED substrate and preparation method of polyimide
A polyimide and substrate technology, applied in the field of material science, can solve problems such as inability to meet, and achieve the effects of compact stacking, regular arrangement, simple and diverse preparation processes
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Embodiment 1
[0039] This example provides the synthesis of 2,7-bis((4-aminophenyl)amino)-9H-xanthen-9-one:
[0040]
[0041] S1. Synthesis of intermediate 2,7-diamino-9H-xanthen-9-one:
[0042] Add 3.54g (0.01mol) of 2,7-dibromo-9H-xanthen-9-one, an appropriate amount of cuprous oxide, 50ml of NMP, and 13ml of ammonia water (29%, 0.2mol) into a 200ml pressure-resistant bottle, protected by argon, at 100 ℃ reaction, after the reaction is completed, the reaction solution is poured into ice water, extracted with dichloromethane, the solvent is removed under reduced pressure, and the product uses dichloromethane:n-hexane=2:1 (volume ratio) as the mobile phase and silica gel as the stationary phase Purified by column chromatography, the product was collected and spin-dried, and dried in vacuum at 80°C for 24h to obtain an intermediate. The intermediate structure is as follows:
[0043]
[0044] S2. Synthesis of intermediate 2,7-bis((4-nitrophenyl)amino)-9H-xanthen-9-one:
[0045]Add 2....
Embodiment 2
[0050] This example provides
[0051] Synthesis of 2-((5-aminopyridin-2-yl)amino)-6-((6-aminopyridin-3-yl)amino)-9H-xanthen-9-one:
[0052]
[0053] S1. Synthesis of intermediate 2,6-diamino-9H-xanthen-9-one:
[0054] Add 3.54g (0.01mol) of 2,6-dibromo-9H-xanthen-9-one, an appropriate amount of cuprous oxide, 50ml of NMP, and 13ml of ammonia water (29%, 0.2mol) into a 200ml pressure-resistant bottle, protected by argon, at 100 ℃ reaction, after the reaction is completed, the reaction solution is poured into ice water, extracted with dichloromethane, the solvent is removed under reduced pressure, and the product uses dichloromethane:n-hexane=2:1 (volume ratio) as the mobile phase and silica gel as the stationary phase Purified by column chromatography, the product was collected and spin-dried, and dried in vacuum at 80°C for 24h to obtain an intermediate. The intermediate structure is as follows:
[0055]
[0056] S2. Synthetic intermediates
[0057] 2-((5-nitropyridi...
Embodiment 3
[0065] This example provides the synthesis of 3,6-bis((3-aminophenyl)amino)-9H-xanthen-9-one:
[0066]
[0067] S1. Synthesis of intermediate 2,6-diamino-9H-xanthen-9-one:
[0068] Add 3.54g (0.01mol) of 2,6-dibromo-9H-xanthen-9-one, an appropriate amount of cuprous oxide, 50ml of NMP, and 13ml of ammonia water (29%, 0.2mol) into a 200ml pressure-resistant bottle, protected by argon, at 100 ℃ reaction, after the reaction is completed, the reaction solution is poured into ice water, extracted with dichloromethane, and the solvent is removed under reduced pressure, the product uses dichloromethane:n-hexane=2:1 (volume ratio) as the mobile phase and silica gel as the stationary phase Purified by column chromatography, the product was collected and spin-dried, and dried in vacuum at 80°C for 24h to obtain an intermediate. The intermediate structure is as follows:
[0069]
[0070] S2. Synthesis of intermediate 3,6-bis((3-nitrophenyl)amino)-9H-xanthen-9-one:
[0071] Add 2...
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